rs1555735545, STRN4;FKRP

N. diseases: 22
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Arachnodactyly
CUI: C0003706
Disease: Arachnodactyly
25 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Chronic fatigue
CUI: C0518656
Disease: Chronic fatigue
2 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Creatine phosphokinase serum increased
CUI: C0241005
Disease: Creatine phosphokinase serum increased
43 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Dyspnea
CUI: C0013404
Disease: Dyspnea
26 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Electrocardiogram abnormal
CUI: C0522055
Disease: Electrocardiogram abnormal
54 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Elevated aldolase level
CUI: C4022858
Disease: Elevated aldolase level
3 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Exercise-induced myoglobinuria
CUI: C1845155
Disease: Exercise-induced myoglobinuria
2 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Gait imbalance
CUI: C1836150
Disease: Gait imbalance
24 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Hyperextensible skin of face
CUI: C4024883
Disease: Hyperextensible skin of face
2 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Intolerant of heat
CUI: C0231274
Disease: Intolerant of heat
7 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
CUI: C1846672
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
52 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Myopia
CUI: C0027092
Disease: Myopia
167 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Pain
CUI: C0030193
Disease: Pain
196 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Palpitations
CUI: C0030252
Disease: Palpitations
7 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Paresthesia
CUI: C0030554
Disease: Paresthesia
8 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Postural hypotension with compensatory tachycardia
CUI: C1850438
Disease: Postural hypotension with compensatory tachycardia
2 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Range of joint movement increased
CUI: C1844820
Disease: Range of joint movement increased
46 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Rhabdomyolysis
CUI: C0035410
Disease: Rhabdomyolysis
15 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
135 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
Vertigo
CUI: C0042571
Disease: Vertigo
35 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0